Overview
Povidone, also known as polyvinylpyrrolidone (PVP) or polyvidone, is a synthetic water-soluble polymer made from the monomer N-vinylpyrrolidone used as a binder in many pharmaceutical tablets and lubricant in eye drops. It is also used in many technical applications with various roles as an adhesive, additive, and emulsifier. When in complex with iodine, Povidone-iodine displays antiseptic properties where the iodine, a bactericidal component, mainly contributes to this effect, and povidone acts as a carrier . Povidone-iodine can be found in over-the-counter topical solutions, ointment, pessaries, liquid soaps and surgical scrubs. The clinical effectiveness of Povidone-iodine on wound healing remains somewhat controversial, as it was demonstrated in a few clinical studies that the application of the compound in wounds was associated with impaired wound healing, reduced wound strength, or infection in open wounds . The FDA withdrew its approval for the use of all intravenous drug products containing povidone. Other formulations of povidone continue to be available.
Indication
When in complex with iodine, indicated for inducing antisepsis for prevention of infection in minor cuts, scrapes, and burns.
Associated Conditions
- Dry Eyes
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2024/02/28 | Phase 4 | Recruiting | Mary K Hayden | ||
2023/02/27 | Phase 4 | Withdrawn | |||
2022/03/18 | Phase 2 | Completed | |||
2021/10/14 | Phase 4 | UNKNOWN | |||
2021/08/25 | Phase 3 | UNKNOWN | |||
2021/01/22 | Phase 4 | Completed | |||
2020/10/27 | Phase 4 | UNKNOWN | |||
2019/08/01 | Phase 1 | UNKNOWN | Farabi Eye Hospital | ||
2018/06/08 | Not Applicable | Completed | |||
2017/01/09 | Phase 4 | UNKNOWN |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
---|---|---|---|---|---|
DLC Laboratories, Inc. | 24286-1575 | OPHTHALMIC | 10 mg in 1 mL | 4/18/2025 | |
Preferred PHarmaceuticals Inc. | 68788-8635 | OPHTHALMIC | 1 g in 100 mL | 5/7/2025 | |
CorneaCare Inc | 82875-003 | OPHTHALMIC | 0.25 g in 100 mL | 8/2/2025 |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
---|---|---|---|
No EMA approvals found for this drug. |
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No HSA approvals found for this drug. |
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
---|---|---|---|---|---|
No NMPA approvals found for this drug. |
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
---|---|---|---|---|---|
No PPB approvals found for this drug. |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
---|---|---|---|---|---|
JSHealth Skin + Digestion | 387956 | Medicine | A | 5/4/2022 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
---|---|---|---|---|---|
VISINE FOR RED EYE COOL | johnson & johnson inc | 02328399 | Drops - Ophthalmic | 1 % / W/V | 4/15/2010 |
VISINE FOR RED EYE WORKPLACE | johnson & johnson inc | 02436086 | Drops - Ophthalmic | 1 % / W/V | 6/3/2016 |
PMS-ARTIFICIAL TEARS PLUS SOL | 00755311 | Liquid - Ophthalmic | .6 % | 12/31/1989 | |
ADVANCED RELIEF EYE DROPS | juno otc inc | 02344319 | Solution - Ophthalmic | 1 % / W/V | 8/30/2010 |
ARTIFICIAL TEARS PLUS | ivax pharmaceuticals incorporated | 02227916 | Solution - Ophthalmic | 0.6 % | 12/10/1996 |
SOOTHE HYDRATION THERAPY | bausch & lomb inc | 02465310 | Drops - Ophthalmic | 2 % / W/V | N/A |
MOISTURE DROPS | bausch & lomb canada inc. | 02131978 | Drops - Ophthalmic | 0.1 % | 12/31/1995 |
ARTIFICIAL TEARS EXTRA | 02229632 | Solution - Ophthalmic | 0.6 % | 5/16/1997 | |
ADVANCED RELIEF EYE DROPS | kc pharmaceuticals inc | 02455293 | Solution - Ophthalmic | 1 % / W/V | N/A |
VISINE FOR RED EYE TRIPLE ACTION | johnson & johnson inc | 02248657 | Drops - Ophthalmic | 1 % / W/V | 3/8/2005 |
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
---|---|---|---|---|---|
OCULOTECT 50 mg/ml COLIRIO EN SOLUCION EN ENVASE UNIDOSIS | Alcon Healthcare S.A. | 61983 | COLIRIO EN SOLUCIÓN | Sin Receta | Not Commercialized |
OCULOTECT 50 MG/ML COLIRIO EN SOLUCION | 1-21275 | COLIRIO EN SOLUCIÓN | Sin Receta | Not Commercialized | |
OCULOTECT 50 mg/ml COLIRIO EN SOLUCION | Alcon Healthcare S.A. | 61982 | COLIRIO EN SOLUCIÓN | Sin Receta | Not Commercialized |
OCULOTECT 50 MG/ML COLIRIO EN SOLUCION | Alcon Portugal Produtos E Equipamentos Oftalmologicos Lda. | 2630085 | COLIRIO EN SOLUCIÓN | Sin Receta | Not Commercialized |
OCULOTECT 50 MG/ML COLIRIO EN SOLUCION EN ENVASE UNIDOSIS | Alcon Portugal Produtos E Equipamentos Oftalmologicos Lda. | 2943389 | COLIRIO EN SOLUCIÓN EN ENVASE UNIDOSIS | Sin Receta | Not Commercialized |
Philippines FDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Philippines FDA approvals found for this drug. |
Saudi SFDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Saudi SFDA approvals found for this drug. |
Malaysia NPRA Drug Approvals
Approved Product | Company | Registration Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Malaysia NPRA approvals found for this drug. |
UK EMC Drug Information
Medicine Name | MA Holder | MA Number | Pharmaceutical Form | Active Ingredient | Authorization Date |
---|---|---|---|---|---|
No UK EMC drug information found for this drug. |
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